Gao Jian, Zhang Wenli, Ehrhardt Anja
Institute for Virology and Microbiology, Center for Biomedical Education and Research (ZBAF), Department of Human Medicine, Faculty of Health, Witten/Herdecke University, 58453 Witten, Germany.
Cancers (Basel). 2020 May 2;12(5):1139. doi: 10.3390/cancers12051139.
Adenoviral vectors (AdVs) have attracted much attention in the fields of vaccine development and treatment for diseases such as genetic disorders and cancer. In this review, we discuss the utility of AdVs in cancer therapies. In recent years, AdVs were modified as oncolytic AdVs (OAs) that possess the characteristics of cancer cell-specific replication and killing. Different carriers such as diverse cells and extracellular vesicles are being explored for delivering OAs into cancer sites after systemic administration. In addition, there are also various strategies to improve cancer-specific replication of OAs, mainly through modifying the early region 1 (E1) of the virus genome. It has been documented that oncolytic viruses (OVs) function through stimulating the immune system, resulting in the inhibition of cancer progression and, in combination with classical immune modulators, the anti-cancer effect of OAs can be even further enforced. To enhance the cancer treatment efficacy, OAs are also combined with other standard treatments, including surgery, chemotherapy and radiotherapy. Adenovirus type 5 (Ad5) has mainly been explored to develop vectors for cancer treatment with different modulations. Only a limited number of the more than 100 identified AdV types were converted into OAs and, therefore, the construction of an adenovirus library for the screening of potential novel OA candidates is essential. Here, we provide a state-of-the-art overview of currently performed and completed clinic trials with OAs and an adenovirus library, providing novel possibilities for developing innovative adenoviral vectors for cancer treatment.
腺病毒载体(AdVs)在疫苗开发以及遗传疾病和癌症等疾病的治疗领域备受关注。在本综述中,我们讨论了腺病毒载体在癌症治疗中的效用。近年来,腺病毒载体被改造为溶瘤腺病毒(OAs),其具有癌细胞特异性复制和杀伤的特性。在全身给药后,人们正在探索不同的载体,如各种细胞和细胞外囊泡,将溶瘤腺病毒递送至癌症部位。此外,还有多种策略来提高溶瘤腺病毒的癌症特异性复制,主要是通过修饰病毒基因组的早期区域1(E1)。据记载,溶瘤病毒(OVs)通过刺激免疫系统发挥作用,从而抑制癌症进展,并且与经典免疫调节剂联合使用时,溶瘤腺病毒的抗癌效果可以进一步增强。为了提高癌症治疗效果,溶瘤腺病毒还与其他标准治疗方法联合使用,包括手术、化疗和放疗。5型腺病毒(Ad5)主要被用于探索开发经过不同调控的癌症治疗载体。在已鉴定的100多种腺病毒类型中,只有少数被转化为溶瘤腺病毒,因此构建一个腺病毒文库以筛选潜在的新型溶瘤腺病毒候选物至关重要。在此,我们提供了一份关于目前正在进行和已经完成的溶瘤腺病毒及腺病毒文库临床试验的最新综述,为开发用于癌症治疗的创新型腺病毒载体提供了新的可能性。